Pages that link to "Frequently Asked Questions (FAQs)"
Jump to navigation
Jump to search
The following pages link to Frequently Asked Questions (FAQs):
Displaying 50 items.
- CNS5:Metastases to the brain and spinal cord parenchyma (← links)
- CNS5:Metastases to the meninges (← links)
- GTS5:Constitutional mismatch repair deficiency (CMMRD) syndrome (MLH1, PMS2, MSH2, MSH6) (← links)
- GTS5:DICER1-related tumour predisposition syndrome (DICER1) (← links)
- GTS5:Neurofibromatosis type 1 (NF1) (← links)
- GTS5:Familial adenomatous polyposis (APC) (← links)
- GTS5:Ataxia-telangiectasia syndrome (ATM) (← links)
- GTS5:Li-Fraumeni syndrome (TP53) (← links)
- GTS5:CHEK2-related hereditary (breast) cancer predisposition syndrome (CHEK2) (← links)
- GTS5:Hereditary gastric and breast cancer syndrome (CDH1, CTNNA1) (← links)
- GTS5:PALB2-related cancer predisposition syndrome (PALB2) (← links)
- GTS5:Peutz-Jeghers syndrome (STK11) (← links)
- GTS5:Fanconi anaemia (FANC genes) (← links)
- GTS5:Bloom syndrome (BLM) (← links)
- GTS5:Von Hippel-Lindau syndrome (VHL) (← links)
- GTS5:Klinefelter syndrome (← links)
- GTS5:Turner syndrome (← links)
- GTS5:Down syndrome (← links)
- GTS5:WAGR syndrome (WT1) (← links)
- GTS5:NF2-related schwannomatosis (NF2) (← links)
- GTS5:Multiple endocrine neoplasia type 2 (RET) (← links)
- GTS5:Multiple endocrine neoplasia type 1 (MEN1) (← links)
- GTS5:PTEN hamartoma tumour syndrome (PTEN) (← links)
- GTS5:SDH-deficient tumour syndrome - Hereditary phaeochromocytoma-paraganglioma syndromes (SDHA, SDHB, SDHC, SDHD, SDHAF2) (← links)
- GTS5:Lynch Syndrome (MLH1, PMS2, MSH2, MSH6) (← links)
- GTS5:Hereditary papillary renal carcinoma (MET) (← links)
- GTS5:Juvenile polyposis syndrome (BMPR1A, SMAD4) (← links)
- GTS5:Hereditary neuroblastoma (ALK, PHOX2B) (← links)
- GTS5:Encephalocraniocutaneous lipomatosis (FGFR1) (← links)
- GTS5:Glucagon cell hyperplasia and neoplasia (GCGR) (← links)
- GTS5:McCune-Albright syndrome (GNAS) (← links)
- GTS5:Sturge-Weber syndrome (GNAQ) (← links)
- GTS5:Costello syndrome (HRAS) (← links)
- GTS5:Noonan syndrome (Various genes) (← links)
- GTS5:Schimmelpenning-Feuerstein-Mims (HRAS, KRAS) (← links)
- GTS5:Carney complex (PRKAR1A, PDE8B, PDE11A) (← links)
- GTS5:PROS syndrome (PIK3CA) (← links)
- GTS5:Gastric Adenocarcinoma and Proximal Polyposis of Stomach - GAPPS (APC promoter) (← links)
- GTS5:AXIN2-associated polyposis (AXIN2) (← links)
- GTS5:Serrated polyposis (RNF43) (← links)
- GTS5:WT1 related tumour predisposition syndrome (WT1) (← links)
- GTS5:Hereditary mixed polyposis syndrome (GREM1) (← links)
- GTS5:Naevoid basal cell carcinoma syndrome - Gorlin syndrome (PTCH1, SUFU, GPR161) (← links)
- GTS5:SMO-related Curry-Jones syndrome (SMO) (← links)
- GTS5:ELP1-related medulloblastoma predisposition syndrome(ELP1) (← links)
- GTS5:Osteochondromatosis (EXT1, EXT2) (← links)
- GTS5:Brooke-Spiegler syndrome (CYLD) (← links)
- GTS5:Tuberous sclerosis (TSC1, TSC1) (← links)
- GTS5:Activated Phosphatidylinositol-3-OH kinase δ Syndrome - APDS (PIK3CD) (← links)
- GTS5:Multiple endocrine neoplasia type 5, MAX related tumours (MAX) (← links)